电合成
法拉第效率
材料科学
电催化剂
产量(工程)
尖晶石
纳米技术
单体
催化作用
电极
电化学
化学物理
面(心理学)
生物量(生态学)
电子结构
退化(生物学)
纳米晶
电子转移
异质结
自旋(空气动力学)
配体(生物化学)
化学工程
聚合物
析氧
氧化还原
反应中间体
钥匙(锁)
反应机理
分解水
作者
Dan Liu,Xiaohui Yang,Zhengyi Qian,Rong Wang,Weiwei Fu,Jian Li,Y LI,Chengyu Wang,Liguang Wang,Yu Wang
摘要
ABSTRACT The electrosynthesis of 2,5‐furandicarboxylic acid (FDCA), a renewable polymer monomer for degradable plastics, represents a promising strategy for biomass upgrading, yet remains fundamentally limited by the challenge of accommodating diverse reaction intermediates involved in the multi‐electron oxidation of 5‐hydroxymethylfurfural (HMF). Here, we demonstrate that facet‐controlled orbital‐degeneracy‐driven spin regulation in spinel NiCo 2 O 4 offers an effective strategy to accelerate the electrosynthesis of FDCA. The exposed (110) facet modifies the orbital splitting of active‐site Co and leads to a lifted Co 3d orbital degeneracy with a moderate‐spin‐associated electronic configuration. This electronic structure balances the adsorption‐desorption behavior of key intermediates and lowers the overall reaction barrier. Such a design enables complete HMF conversion with a 99.9% yield for FDCA, while an integrated NiCo 2 O 4 nanoarrays electrode with exposed (110) facets delivers Faradaic efficiencies of ∼94% under industrial‐level current densities, underscoring their scalability. These results establish a mechanistic framework for orbital–spin engineering in electrocatalyst design, offering broad implications for accelerating complex multi‐electron transfer reactions.
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